CN115975423B - Reduced graphene oxide/aluminum anti-corrosion material, and preparation method and application thereof - Google Patents
Reduced graphene oxide/aluminum anti-corrosion material, and preparation method and application thereof Download PDFInfo
- Publication number
- CN115975423B CN115975423B CN202310081491.6A CN202310081491A CN115975423B CN 115975423 B CN115975423 B CN 115975423B CN 202310081491 A CN202310081491 A CN 202310081491A CN 115975423 B CN115975423 B CN 115975423B
- Authority
- CN
- China
- Prior art keywords
- graphene oxide
- reduced graphene
- aluminum
- mixed solution
- deionized water
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 114
- 229910021389 graphene Inorganic materials 0.000 title claims abstract description 101
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 46
- 239000000463 material Substances 0.000 title claims abstract description 45
- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 43
- 238000002360 preparation method Methods 0.000 title claims abstract description 22
- 238000005260 corrosion Methods 0.000 title abstract description 31
- 239000011248 coating agent Substances 0.000 claims abstract description 43
- 238000000576 coating method Methods 0.000 claims abstract description 43
- 238000010438 heat treatment Methods 0.000 claims abstract description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 27
- 239000008367 deionised water Substances 0.000 claims abstract description 25
- 229910021641 deionized water Inorganic materials 0.000 claims abstract description 25
- 238000005096 rolling process Methods 0.000 claims abstract description 24
- 239000012298 atmosphere Substances 0.000 claims abstract description 13
- 239000002131 composite material Substances 0.000 claims abstract description 6
- 238000001704 evaporation Methods 0.000 claims abstract description 6
- 239000002904 solvent Substances 0.000 claims abstract description 6
- 230000001154 acute effect Effects 0.000 claims abstract description 3
- 239000011259 mixed solution Substances 0.000 claims description 25
- 239000000243 solution Substances 0.000 claims description 20
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical group [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 15
- 238000003756 stirring Methods 0.000 claims description 15
- 229910002804 graphite Inorganic materials 0.000 claims description 13
- 239000010439 graphite Substances 0.000 claims description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 12
- 238000001035 drying Methods 0.000 claims description 10
- 239000005457 ice water Substances 0.000 claims description 10
- -1 polytetrafluoroethylene Polymers 0.000 claims description 10
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims description 10
- 239000004810 polytetrafluoroethylene Substances 0.000 claims description 10
- 229910052786 argon Inorganic materials 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 238000005498 polishing Methods 0.000 claims description 8
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 claims description 8
- 239000000758 substrate Substances 0.000 claims description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- 230000009467 reduction Effects 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 238000005406 washing Methods 0.000 claims description 5
- 239000007789 gas Substances 0.000 claims description 4
- 239000011261 inert gas Substances 0.000 claims description 4
- 239000012286 potassium permanganate Substances 0.000 claims description 4
- 239000004317 sodium nitrate Substances 0.000 claims description 4
- 235000010344 sodium nitrate Nutrition 0.000 claims description 4
- 238000007605 air drying Methods 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 2
- 230000035484 reaction time Effects 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 239000011159 matrix material Substances 0.000 abstract description 14
- 239000010410 layer Substances 0.000 abstract description 9
- 239000011229 interlayer Substances 0.000 abstract description 7
- 230000001105 regulatory effect Effects 0.000 abstract description 3
- 239000006185 dispersion Substances 0.000 abstract description 2
- 239000002086 nanomaterial Substances 0.000 abstract description 2
- 230000007797 corrosion Effects 0.000 description 20
- 239000000203 mixture Substances 0.000 description 11
- 239000000919 ceramic Substances 0.000 description 6
- 239000002244 precipitate Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 239000000523 sample Substances 0.000 description 5
- 230000008901 benefit Effects 0.000 description 4
- 244000137852 Petrea volubilis Species 0.000 description 3
- 239000012300 argon atmosphere Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000004108 freeze drying Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000010287 polarization Effects 0.000 description 3
- 238000010008 shearing Methods 0.000 description 3
- 238000009210 therapy by ultrasound Methods 0.000 description 3
- 238000005303 weighing Methods 0.000 description 3
- 239000002390 adhesive tape Substances 0.000 description 2
- 239000012496 blank sample Substances 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 238000000840 electrochemical analysis Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000011253 protective coating Substances 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005536 corrosion prevention Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000001878 scanning electron micrograph Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000009777 vacuum freeze-drying Methods 0.000 description 1
Abstract
The invention belongs to the technical field of preparation of corrosion-protection nano materials, and particularly relates to a reduced graphene oxide/aluminum anti-corrosion material, a preparation method and application thereof. The preparation method of the reduced graphene oxide/aluminum anticorrosive material comprises the following steps: ultrasonically dispersing graphene oxide in deionized water, coating, evaporating a solvent, and heating under an inert and reducing mixed atmosphere to obtain a reduced graphene oxide film; and removing the surface oxide layer of the right-angle aluminum matrix with the acute angle of 35-50 degrees, attaching the reduced graphene oxide film to the inclined edge of the aluminum matrix, performing heat treatment under inert atmosphere, and rolling to obtain the anticorrosive coating composite material with the reduced graphene oxide. The invention solves the problems that the existing graphene/aluminum anti-corrosion material has low bonding strength with a matrix, the interlayer spacing of the graphene cannot be regulated and reduced, the dispersion of the graphene is uneven and the preparation process is complex.
Description
Technical Field
The invention belongs to the technical field of preparation of corrosion-protection nano materials, and particularly relates to a reduced graphene oxide/aluminum anti-corrosion material, a preparation method and application thereof.
Background
Aluminum metal is widely applied to various fields of industrial manufacture, and has the advantages of light weight, high conductivity and the like; a layer of aluminum oxide naturally exists on the surface of aluminum, so that a certain anti-corrosion protection effect is achieved, however, the naturally-formed protective layer is sparse, and the protective effect is lost under the conditions of acidity and alkalinity, so that the requirements of people cannot be met. Therefore, improving the corrosion resistance of aluminum metal is a key point for further expanding the application range and developing the light weight of aluminum metal.
Graphene as an sp 2 Hybrid two-dimensional materials, which have excellent corrosion resistance due to their in-plane impermeability to almost all molecules, have been regarded as popular research materials in the field of corrosion protection, but graphene applications still have the following problems: firstly, graphene has stable chemical properties and is difficult to react with a metal matrix, so that the bonding strength of a coating and an aluminum matrix is low, and the integrity of the graphene is easily damaged by a method of improving the bonding strength by applying deformation force in a traditional processing mode, so that a new problem of losing the protective effect of the coating occurs; secondly, small molecular substances can permeate into the graphene interlayer gaps to cause failure of corrosion protection, and the traditional method cannot regulate and control the interlayer spacing of the graphene, so that the problem cannot be avoided, and the application of the graphene in the field of corrosion protection is severely restricted.
Therefore, the design and development of the graphene/aluminum anticorrosive material which can be directly combined with the aluminum matrix at high strength and can regulate and control the interlayer spacing of the reduced graphene is of great significance.
Disclosure of Invention
Aiming at the defects of the prior art, the invention provides a reduced graphene oxide/aluminum anti-corrosion material, and a preparation method and application thereof, so as to solve the problems that the existing graphene/aluminum anti-corrosion material has low bonding strength with a matrix, the spacing between graphene layers cannot be regulated and reduced, the dispersion of graphene is uneven, and the preparation process is complex. The preparation method provided by the invention has the advantages of simplicity, high efficiency, environment-friendly production process and excellent corrosion protection effect.
In order to achieve the above purpose, the technical scheme of the invention is as follows:
the preparation method of the reduced graphene oxide/aluminum anticorrosive material is characterized by comprising the following steps of:
(1) Ultrasonically dispersing graphene oxide in deionized water to obtain a graphene oxide solution;
(2) Coating the graphene oxide solution in the step (1) and evaporating a solvent to obtain a graphene oxide film;
(3) Heating the graphene oxide film in the step (2) under an inert and reducing mixed atmosphere to obtain a reduced graphene oxide film;
(4) And (3) removing a surface oxide layer from the right-angle aluminum matrix with the acute angle of 35-50 degrees, attaching the reduced graphene oxide film in the step (3) to the inclined edge of the aluminum matrix, performing heat treatment in an inert gas atmosphere, and rolling to obtain the composite material with the reduced graphene oxide anticorrosive coating.
Preferably, the graphene oxide of the step (1) is prepared according to the following steps:
s1, mixing graphite, sodium nitrate and concentrated sulfuric acid, stirring in an ice-water bath for reaction for 15-45min, and controlling the temperature at 0-10 ℃ during the period to obtain a mixed solution A;
wherein, the volume ratio of the mass of graphite to the mass of sodium nitrate to the volume of sulfuric acid is 2g: (1-2) g: (46-69) mL, wherein the volume fraction of the concentrated sulfuric acid is 98%, the graphite is 200 meshes or 325 meshes, and the stirring speed is 200-400rpm;
s2, adding potassium permanganate into the mixed solution A, continuing to stir in an ice-water bath for reaction for 4-6 hours, then raising the temperature to 35+/-3 ℃ and reacting for 0.5-1 hour to obtain a mixed solution B;
wherein, the mass ratio of potassium permanganate to graphite is 6:2;
s3, dropwise adding deionized water into the mixed solution B, heating to 100 ℃ and reacting for 20-40min, and stopping reacting to obtain a mixed solution C;
wherein the volume ratio of the deionized water to the mixed solution B is 1.8-2:1, a step of;
s4, dropwise adding deionized water into the mixed solution C under the stirring condition, and then adding H 2 O 2 Stopping stirring, standing, centrifuging, adding dilute hydrochloric acid into the solid, centrifuging, washing with water, and drying to obtain graphene oxide;
wherein the volume ratio of the deionized water to the mixed solution C is 1.8-2.4:1 deionized water and H 2 O 2 The volume ratio of (2) is 12-26:1, a step of; the volume fraction of the diluted hydrochloric acid is 3-6%, the centrifugation speed is 4000-8000rpm, the centrifugation time is 5-10min, and the drying mode is vacuum drying, freeze drying or forced air drying.
Preferably, the concentration of the graphene oxide solution in the step (1) is 2-2000mg/mL.
Preferably, the method for coating and evaporating the solvent in the step (2) is as follows: and (3) polishing the polytetrafluoroethylene plate, enclosing a square frame on the surface of the polytetrafluoroethylene plate, dripping the graphene oxide solution obtained in the step (1) into the square frame, and drying to obtain the graphene oxide film.
Preferably, the side length of the square frame is 4-8cm, and the thickness of the frame is 0.5-2mm;
the dripping volume is 5-10mL, the drying mode is forced air drying, the temperature is 40-70 ℃ and the time is 2-4h.
Preferably, in the step (3), the inert atmosphere is argon, nitrogen or a mixed gas of the argon and the nitrogen, and the reducing atmosphere is hydrogen; the heating temperature is 400-800 ℃, and the reaction time is 5-30min.
Preferably, the inert gas in the step (4) is argon, nitrogen or a mixed gas of the argon and the nitrogen; the heat treatment temperature is 200-500 ℃ and the time is 1-2h.
Preferably, the rolling reduction in the step (4) is 50-80%, and the rolling roller speed is 50-200r/min.
The invention also protects the reduced graphene oxide/aluminum anticorrosive material prepared by the preparation method.
The invention also protects the application of the reduced graphene oxide/aluminum anticorrosive material in preparing ocean navigation anticorrosive material, and the application method comprises the following steps: the application method comprises the following steps: firstly, coating a reduced graphene oxide/aluminum anticorrosive material, evaporating a solvent to obtain a uniform coating, uniformly coating the coating on the surface of pure aluminum or aluminum alloy material, and combining the whole after rolling processing deformation to obtain the anticorrosive coating.
Compared with the prior art, the invention has the beneficial effects that:
1. according to the invention, the triangular aluminum matrix is utilized for rolling with an inclined angle, namely shear rolling (shear-rolling), so that the material is prepared, the interface bonding strength of the film and the aluminum matrix is improved, the middle layer required by the traditional method is replaced, and the method is environment-friendly and efficient. The method reduces the interlayer spacing of the rGO film while realizing the combination of the coating and the matrix, improves the corrosion resistance of the rGO film, combines the rolling forming and the shearing separation and the melting into one step, has the advantages of short flow and high efficiency, and has higher industrial production potential.
2. The reason for regulating and controlling the interlayer spacing of the graphene is as follows: the rolling force provided by the shearing rolling enables the graphene layers to deform and be compressed, the arrangement is tighter, and the interlayer spacing is reduced.
3. The reduced graphene oxide coating and the aluminum substrate have high bonding strength, and the reason is that: the rolling deformation force in the shearing rolling process is applied to the joint of the coating and the aluminum matrix, so that the bonding effect is improved, and the bonding strength is enhanced.
Drawings
FIG. 1 is a flow chart of the preparation of a material with a reduced graphene oxide corrosion protection coating according to the present invention;
FIG. 2 is a schematic view of a shear rolling process according to an embodiment of the present invention;
FIG. 3 is a graph comparing polarization curves of the reduced graphene oxide anti-corrosion coating material prepared in example 1 of the present invention with the non-anti-corrosion coating material;
FIG. 4 is a cross-sectional scanning electron micrograph of the reduced graphene oxide/graphite anti-corrosion coating material prepared in example 2 of the present invention;
FIG. 5 is a schematic illustration of the corrosion process of the reduced graphene oxide/graphite corrosion-protective coating material and the non-corrosion-protective coating material prepared in example 2 of the present invention.
Detailed Description
The following detailed description of specific embodiments of the invention is, but it should be understood that the invention is not limited to specific embodiments. All other embodiments, which can be made by those skilled in the art based on the embodiments of the invention without making any inventive effort, are intended to be within the scope of the invention. The experimental methods described in the examples of the present invention are conventional methods unless otherwise specified.
Example 1
The preparation method of the 45-degree inclined plane coated reduced graphene oxide anticorrosive material comprises the following steps:
(1) Preparation of graphene oxide using the modified hummers method: weigh 2g graphite, 1g NaNO 3 Respectively adding into a three-hole flask, and measuring 46ml98% H 2 SO 4 Adding the mixture into a three-hole flask, placing the three-hole flask into an ice-water bath, adding a magneton, and stirring and reacting for 30min at a rotating speed of 200rpm to obtain a mixed solution A;
weigh 6gKMnO 4 Slowly adding the mixture into the mixture A at a constant speed, maintaining an ice water bath, reacting for 5 hours, heating to 32 ℃, and reacting for 30 minutes to obtain a mixture B;
adding 98mL of deionized water into the flask dropwise at a constant speed, heating to 100 ℃ for reacting for 20min, and stopping heating to obtain a mixed solution C;
280mL of deionized water was added dropwise to the mixture C at a constant rate, followed by 15mLH to the flask 2 O 2 Stopping stirring, adding the liquid into a centrifuge tube, centrifuging at 4000rpm for 5min, adding 4vol% HCl into the lower precipitate, centrifuging at 4000rpm for 5min, washing the lower precipitate with deionized water for 5-6 times, and freeze-drying for 72h to obtain GO;
(2) Preparing a graphene oxide film: weighing 0.2g of prepared GO, placing in a beaker, adding 30mL of deionized water, carrying out ultrasonic treatment at normal temperature for 2 hours to uniformly disperse to obtain a graphene oxide solution with the concentration of 6.67mg/mL, polishing a polytetrafluoroethylene plate, adhering an adhesive tape to enclose a square frame with the side length of 5cm and the frame thickness of 1mm, sucking 5mL of the obtained graphene oxide solution, slowly dripping the 5mL of the graphene oxide solution into the square frame of the polytetrafluoroethylene plate, and drying at 60 ℃ for 4 hours to obtain a GO film;
(3) Preparing a reduced graphene oxide film: putting the obtained GO film into a ceramic ark, putting the ceramic ark into a tube furnace, heating to 400 ℃ under the mixed atmosphere of argon and hydrogen, reacting for 30min at a heating rate of 5 ℃/min, cooling to room temperature along with the furnace, and taking out to obtain the rGO film;
(4) Preparing a reduced graphene oxide anticorrosive coating material: and (3) polishing the aluminum block by using sand paper to remove a surface oxide layer, coating the rGO film obtained in the step (3) on a 45-degree inclined plane right-angle aluminum substrate, performing heat treatment for 1h at 400 ℃ in an argon atmosphere, wherein the rolling reduction rate is 80%, the rotating speed of a roller is 100r/min, and separating the material along the middle of the film after rolling to obtain the composite material with the reduced graphene oxide anticorrosive coating.
Taking a blank sample (without coating) and coating the blank sample with the reduced graphene oxide coating at 0.5MH 2 SO 4 Performing three-electrode electrochemical test in the solution, wherein the reference electrode is Ag/AgCl, the counter electrode is Pt electrode, and the working electrode is 1cm 2 The measured polarization curve data is shown in figure 3. The white sample in the graph is a black curve, the sample coated with the reduced graphene oxide coating is a gray curve, the x-axis is a voltage value, the y-axis is the absolute value of current and takes the logarithm, the voltage represents the corrosion sensitivity of the material, the closer the value is to 0, the lower the sensitivity is, the current represents the corrosion intensity of the material, the smaller the current represents the better the corrosion resistance, the lower the comprehensive representation is in the graph, the better the corrosion resistance of the material is, and therefore, the corrosion potential and the corrosion current of the sample are obviously reduced by the coating, and the excellent corrosion protection effect is achieved.
Example 2
The preparation method of the 35-degree inclined plane coated reduced graphene oxide anticorrosive coating material is the same as that of example 1, and the only difference is that: in the step (4), a 35-degree inclined plane right-angle aluminum substrate is adopted, and the rolling reduction is 70%.
Example 3
The preparation of the 50-degree inclined plane coated reduced graphene oxide anticorrosive material comprises the following steps:
(1) Preparation of graphene oxide using the modified hummers method: weigh 2g graphite, 1.5g NaNO 3 Respectively adding into a three-hole flask, and measuring 47ml98% H 2 SO 4 Adding the mixture into a three-hole flask, placing the three-hole flask into an ice-water bath, adding a magneton, and stirring and reacting for 15min at a rotating speed of 300rpm to obtain a mixed solution A;
weigh 6gKMnO 4 Slowly adding the mixture into the mixture A at a constant speed, maintaining an ice water bath, reacting for 4 hours, increasing the temperature to 38 ℃, and reacting for 1 hour to obtain a mixture B;
adding 98mL of deionized water into the flask dropwise at a constant speed, heating to 100 ℃ for reaction for 30min, and stopping heating to obtain a mixed solution C;
into the mixed solution C280mL of deionized water was added dropwise at a constant rate to the flask followed by 15mLH to the flask 2 O 2 Stopping stirring, adding the liquid into a centrifuge tube, centrifuging at 6000rpm for 8min, adding 3vol% HCl into the lower precipitate, centrifuging at 6000rpm for 8min, washing the lower precipitate with deionized water for 5-6 times, and freeze-drying for 72h to obtain GO;
(2) Preparing a graphene oxide film: weighing 0.06g of prepared GO, placing in a beaker, adding 30mL of deionized water, carrying out ultrasonic treatment at normal temperature for 2 hours to uniformly disperse to obtain a graphene oxide solution with the concentration of 2mg/mL, polishing a polytetrafluoroethylene plate, enclosing a tape to form a square frame with the side length of 4cm and the frame thickness of 0.5mm, sucking 5mL of the obtained graphene oxide solution, slowly dripping the 5mL of the graphene oxide solution into the square frame of the polytetrafluoroethylene plate, and drying at 70 ℃ for 2 hours to obtain a GO film;
(3) Preparing a reduced graphene oxide film: putting the obtained GO film into a ceramic ark, putting the ceramic ark into a tube furnace, heating to 600 ℃ under the mixed atmosphere of argon and hydrogen, reacting for 15min at a heating rate of 5 ℃/min, cooling to room temperature along with the furnace, and taking out to obtain the rGO film;
(4) Preparing a reduced graphene oxide anticorrosive coating material: and (3) polishing the aluminum block by using sand paper to remove a surface oxide layer, coating the rGO film obtained in the step (3) on a 50-DEG inclined plane right-angle aluminum substrate, performing heat treatment for 1.5 hours at 200 ℃ in an argon atmosphere, wherein the rolling reduction rate is 60%, the rotating speed of a roller is 50r/min, and separating the material along the middle of the film after rolling to obtain the composite material with the reduced graphene oxide anticorrosive coating.
Example 4
The preparation of the 40-DEG inclined plane coated reduced graphene oxide anticorrosive material comprises the following steps:
(1) Preparation of graphene oxide using the modified hummers method: weigh 2g graphite, 1g NaNO 3 Respectively adding into a three-hole flask, and measuring 48ml98% H 2 SO 4 Adding the mixture into a three-hole flask, placing the three-hole flask into an ice-water bath, adding a magneton, and stirring and reacting for 45min at a rotating speed of 400rpm to obtain a mixed solution A;
weigh 6gKMnO 4 Slowly adding into the mixed solution A at constant speed, maintaining ice-water bath, reacting for 6 hr, and increasing temperature to 35 deg.CReacting for 1h to obtain a mixed solution B;
adding 98mL of deionized water into the flask dropwise at a constant speed, heating to 100 ℃ for reaction for 40min, and stopping heating to obtain a mixed solution C;
280mL of deionized water was added dropwise to the mixture C at a constant rate, followed by 15mLH to the flask 2 O 2 Stopping stirring, adding the liquid into a centrifuge tube, centrifuging at 8000rpm for 5min, adding 6vol% HCl into the lower precipitate, centrifuging at 8000rpm for 5min, washing the lower precipitate with deionized water for 5-6 times, and freeze-drying for 72h to obtain GO;
(2) Preparing a graphene oxide film: weighing 60g of prepared GO, placing in a beaker, adding 30mL of deionized water, carrying out ultrasonic treatment at normal temperature for 2 hours to uniformly disperse to obtain graphene oxide solution with the concentration of 2000mg/mL, polishing a polytetrafluoroethylene plate, adhering an adhesive tape to enclose a square frame with the side length of 8cm and the frame thickness of 2mm, sucking 5mL of the obtained graphene oxide solution, slowly dripping the 5mL of the graphene oxide solution into the square frame of the polytetrafluoroethylene plate, and drying at 40 ℃ for 4 hours to obtain a GO film;
(3) Preparing a reduced graphene oxide film: putting the obtained GO film into a ceramic ark, putting the ceramic ark into a tube furnace, heating to 800 ℃ under the mixed atmosphere of argon and hydrogen, reacting for 5min at a heating rate of 5 ℃/min, cooling to room temperature along with the furnace, and taking out to obtain the rGO film;
(4) Preparing a reduced graphene oxide anticorrosive coating material: and (3) polishing the aluminum block by using sand paper to remove a surface oxide layer, coating the rGO film obtained in the step (3) on a 40-DEG inclined plane right-angle aluminum substrate, performing heat treatment for 1h at 500 ℃ in an argon atmosphere, wherein the rolling reduction rate is 50%, the rotating speed of a roller is 200r/min, and separating the material along the middle of the film after rolling to obtain the composite material with the reduced graphene oxide anticorrosive coating.
As can be seen from the graph of fig. 4, the resulting material, the corrosion protection coating, is preserved intact and the coating bonds well to the substrate. The test coating sample was taken at 0.5MH 2 SO 4 Three-electrode electrochemical test is carried out in the solution to obtain polarization curve data, the data are processed to obtain a coating, the corrosion potential and the corrosion current of the sample are reduced, as shown in figure 5, the reduced graphene oxide coating in (1)The reaction and corrosion of ions in the solution and the aluminum matrix are blocked, and the corrosion prevention effect is achieved; while the coating has the advantage of low cost.
It will be apparent to those skilled in the art that various modifications and variations can be made to the present invention without departing from the spirit or scope of the invention. Thus, it is intended that the present invention also include such modifications and alterations insofar as they come within the scope of the appended claims or the equivalents thereof.
Claims (8)
1. The preparation method of the reduced graphene oxide/aluminum anticorrosive material is characterized by comprising the following steps of:
(1) Ultrasonically dispersing graphene oxide in deionized water to obtain a graphene oxide solution;
(2) Coating the graphene oxide solution in the step (1) and evaporating a solvent to obtain a graphene oxide film;
(3) Heating the graphene oxide film in the step (2) under an inert and reducing mixed atmosphere to obtain a reduced graphene oxide film;
(4) Removing a surface oxide layer from a right-angle aluminum substrate with an acute angle of 35-50 degrees, attaching the reduced graphene oxide film obtained in the step (3) to the inclined edge of the aluminum substrate, performing heat treatment in an inert gas atmosphere, and rolling to obtain a composite material with the reduced graphene oxide anticorrosive coating;
the rolling reduction rate in the step (4) is 50-80%, and the rolling roller speed is 50-200r/min.
2. The reduced graphene oxide/aluminum anticorrosive material according to claim 1, wherein the graphene oxide of step (1) is prepared according to the following steps:
s1, mixing graphite, sodium nitrate and concentrated sulfuric acid, stirring in an ice-water bath for reaction for 15-45min, and controlling the temperature at 0-10 ℃ during the period to obtain a mixed solution A;
wherein, the volume ratio of the mass of graphite to the mass of sodium nitrate to the volume of sulfuric acid is 2g: (1-2) g: (46-69) mL, wherein the volume fraction of the concentrated sulfuric acid is 98%, and the graphite is 200 meshes or 325 meshes;
s2, adding potassium permanganate into the mixed solution A, continuing to stir in an ice-water bath for reaction for 4-6 hours, then raising the temperature to 35+/-3 ℃ and reacting for 0.5-1 hour to obtain a mixed solution B;
wherein, the mass ratio of potassium permanganate to graphite is 6:2;
s3, dropwise adding deionized water into the mixed solution B, heating to 100 ℃ and reacting for 20-40min, and stopping reacting to obtain a mixed solution C;
wherein the volume ratio of the deionized water to the mixed solution B is 1.8-2:1, a step of;
s4, dropwise adding deionized water into the mixed solution C under the stirring condition, and then adding H 2 O 2 Stopping stirring, standing, centrifuging, adding dilute hydrochloric acid into the solid, centrifuging, washing with water, and drying to obtain graphene oxide;
wherein the volume ratio of the deionized water to the mixed solution C is 1.8-2.4:1 deionized water and H 2 O 2 The volume ratio of (2) is 12-26:1, a step of; the volume fraction of the dilute hydrochloric acid is 3-6%.
3. The method for producing a reduced graphene oxide/aluminum anticorrosive material according to claim 1, wherein the concentration of the graphene oxide solution in the step (1) is 2 to 2000mg/mL.
4. The method for preparing the reduced graphene oxide/aluminum anticorrosive material according to claim 1, wherein the method for coating and evaporating the solvent in the step (2) is as follows: and (3) polishing the polytetrafluoroethylene plate, enclosing a square frame on the surface of the polytetrafluoroethylene plate, dripping the graphene oxide solution obtained in the step (1) into the square frame, and drying to obtain the graphene oxide film.
5. The method for preparing the reduced graphene oxide/aluminum anticorrosive material according to claim 4, wherein the square frame has a side length of 4-8cm and a frame thickness of 0.5-2mm;
the dripping volume is 5-10mL, the drying mode is forced air drying, the temperature is 40-70 ℃ and the time is 2-4h.
6. The method for producing a reduced graphene oxide/aluminum anticorrosive material according to claim 1, wherein in the step (3), the inert atmosphere is argon, nitrogen or a mixed gas of the two, and the reducing atmosphere is hydrogen; the heating temperature is 400-800 ℃, and the reaction time is 5-30min.
7. The method for producing a reduced graphene oxide/aluminum anticorrosive material according to claim 1, wherein the inert gas in the step (4) is argon, nitrogen or a mixed gas of both; the heat treatment temperature is 200-500 ℃ and the time is 1-2h.
8. A reduced graphene oxide/aluminum anticorrosive material produced by the production method according to any one of claims 1 to 7.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202310081491.6A CN115975423B (en) | 2023-02-08 | 2023-02-08 | Reduced graphene oxide/aluminum anti-corrosion material, and preparation method and application thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202310081491.6A CN115975423B (en) | 2023-02-08 | 2023-02-08 | Reduced graphene oxide/aluminum anti-corrosion material, and preparation method and application thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN115975423A CN115975423A (en) | 2023-04-18 |
| CN115975423B true CN115975423B (en) | 2024-02-27 |
Family
ID=85964914
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202310081491.6A Active CN115975423B (en) | 2023-02-08 | 2023-02-08 | Reduced graphene oxide/aluminum anti-corrosion material, and preparation method and application thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN115975423B (en) |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4874627A (en) * | 1988-06-14 | 1989-10-17 | Nouevelle Ice Cream Corporation | Non-fat dairy compositions |
| CN1060947A (en) * | 1990-11-01 | 1992-05-13 | 石河子市牛奶公司 | The preparation method of strawberry sour milk |
| KR20140010552A (en) * | 2012-07-13 | 2014-01-27 | 한국기계연구원 | Spin coating method for coating stainless steel with graphene oxide or reduced graphene oxide and the staninless steel coated with graphene oxide or reduced graphene oxide thereof |
| CN103935103A (en) * | 2014-04-04 | 2014-07-23 | 中国航空工业集团公司北京航空材料研究院 | Preparation method of graphene/metal composite panel |
| CN105695788A (en) * | 2016-04-08 | 2016-06-22 | 上海和伍复合材料有限公司 | Graphene strengthening nickel base composite material and preparing method thereof |
| CN107311659A (en) * | 2017-06-22 | 2017-11-03 | 李若明 | A kind of preparation method of graphite film/graphene composite film |
| WO2018113699A1 (en) * | 2016-12-23 | 2018-06-28 | 北京赛特石墨烯科技有限公司 | Method for preparing anticorrosion graphene composite coating for metal |
| KR102374445B1 (en) * | 2020-11-06 | 2022-03-15 | 한국과학기술연구원 | Method for preparing block copolymer film aligned horizontally in one direction and block copolymer film prepared using the same |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9236156B2 (en) * | 2013-10-18 | 2016-01-12 | Snu R&Db Foundation | Preparing method of reduced graphene oxide film using a chemical reduction method and a pressure-assisted thermal reduction method, reduced graphene oxide film prepared by the same, and graphene electrode including the reduced graphene oxide film |
| US20220140313A1 (en) * | 2014-11-17 | 2022-05-05 | Imagine Intelligent Materials Limited | Graphene Electrode |
| CN108203091B (en) * | 2017-01-23 | 2019-01-18 | 常州富烯科技股份有限公司 | A method of continuously preparing graphene heat conducting film |
| US11542411B2 (en) * | 2017-05-27 | 2023-01-03 | Hangzhou Gaoxi Technology Co., Ltd. | Method for preparing composites on basis of graphene bonding |
| SE541565C2 (en) * | 2018-02-16 | 2019-11-05 | Munksjoe Ahlstrom Oyj | Graphene and graphene paper and its manufacture |
| CN112408385B (en) * | 2019-08-22 | 2021-08-27 | 常州富烯科技股份有限公司 | Graphene oxide slurry with low viscosity and preparation method thereof, graphene oxide film and preparation method thereof |
| US11923526B2 (en) * | 2020-05-11 | 2024-03-05 | Global Graphene Group, Inc. | Process for producing graphene-protected metal foil current collector for a battery or supercapacitor |
-
2023
- 2023-02-08 CN CN202310081491.6A patent/CN115975423B/en active Active
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4874627A (en) * | 1988-06-14 | 1989-10-17 | Nouevelle Ice Cream Corporation | Non-fat dairy compositions |
| CN1060947A (en) * | 1990-11-01 | 1992-05-13 | 石河子市牛奶公司 | The preparation method of strawberry sour milk |
| KR20140010552A (en) * | 2012-07-13 | 2014-01-27 | 한국기계연구원 | Spin coating method for coating stainless steel with graphene oxide or reduced graphene oxide and the staninless steel coated with graphene oxide or reduced graphene oxide thereof |
| CN103935103A (en) * | 2014-04-04 | 2014-07-23 | 中国航空工业集团公司北京航空材料研究院 | Preparation method of graphene/metal composite panel |
| CN105695788A (en) * | 2016-04-08 | 2016-06-22 | 上海和伍复合材料有限公司 | Graphene strengthening nickel base composite material and preparing method thereof |
| WO2018113699A1 (en) * | 2016-12-23 | 2018-06-28 | 北京赛特石墨烯科技有限公司 | Method for preparing anticorrosion graphene composite coating for metal |
| CN107311659A (en) * | 2017-06-22 | 2017-11-03 | 李若明 | A kind of preparation method of graphite film/graphene composite film |
| KR102374445B1 (en) * | 2020-11-06 | 2022-03-15 | 한국과학기술연구원 | Method for preparing block copolymer film aligned horizontally in one direction and block copolymer film prepared using the same |
Also Published As
| Publication number | Publication date |
|---|---|
| CN115975423A (en) | 2023-04-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Chen et al. | Graphene oxide-deposited carbon fiber/cement composites for electromagnetic interference shielding application | |
| CN107353017B (en) | Graphene-coated aluminum oxide ceramic powder and preparation method and application thereof | |
| Tan et al. | Enhanced thermal conductivity in diamond/aluminum composites with a tungsten interface nanolayer | |
| WO2017128929A1 (en) | Method for preparing graphene dispersion and article thereof | |
| JP5951014B2 (en) | Porous film silicon negative electrode material in high performance lithium ion battery and method for producing the same | |
| Li et al. | Electrochemical exfoliation of two-dimensional layered black phosphorus and applications | |
| Domingues et al. | Reduction of graphene oxide films on Al foil for hybrid transparent conductive film applications | |
| EP3601162B1 (en) | A method for the manufacture of graphene oxide from kish graphite | |
| CN103451670B (en) | A kind of Electrochemical preparation method of Graphene | |
| CN105836804B (en) | A kind of graded structure carbon intercalation MoS2@rGO preparation method | |
| WO2014032399A1 (en) | Method for low-temperature preparation of graphene and of graphene-based composite material | |
| CN108559861A (en) | A method of preparing graphene reinforced aluminum matrix composites | |
| CN108264041A (en) | Graphene oxide/copper oxide composite powder and preparation method thereof, microcosmic stratiform structure graphite alkene/method of manufacturing carbon/carbon-copper composite material | |
| CN115975423B (en) | Reduced graphene oxide/aluminum anti-corrosion material, and preparation method and application thereof | |
| Inman et al. | Shear delamination of multilayer MXenes | |
| CN111559743A (en) | Preparation method and application of graphene powder | |
| JP2012096937A (en) | Thermally conductive sheet and method for manufacturing the same | |
| CN110117810B (en) | Method for preparing modified graphene oxide aluminum composite heat conduction material through electrophoresis | |
| Pisarevskaya et al. | Studies of chemical stage of synthesis of electroactive composite based on poly-o-phenylenediamine and graphene oxide | |
| CN109524170A (en) | A kind of preparation method of graphene and fluorin-doped tin oxide transparent conductive film | |
| CN111321314B (en) | Preparation method of graphene reinforced aluminum matrix composite with strong interface bonding strength | |
| CN114572971A (en) | Method for preparing graphene on surface of copper powder | |
| JP2004091251A (en) | Method for reducing thin-film particle having framework comprising carbon | |
| Wang et al. | Electrodeposition of ZnO on carbon nanofiber buckypaper | |
| Hung et al. | Investigation of electrochemical reduction effects on graphene oxide powders for high-performance supercapacitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |